(Q49159530)

18 February 2018

title

Expression of the Sox10 gene during mouse inner ear development. (English)

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18 February 2018

author name string

Watanabe K

1

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18 February 2018

Takeda K

2

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18 February 2018

Katori Y

3

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18 February 2018

Ikeda K

4

1 reference

18 February 2018

Oshima T

5

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18 February 2018

Yasumoto K

6

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18 February 2018

Saito H

7

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18 February 2018

Takasaka T

8

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18 February 2018

Shibahara S

9

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18 February 2018

publication date

1 December 2000

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18 February 2018

published in

Molecular Brain Research

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18 February 2018

volume

84

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18 February 2018

issue

1-2

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18 February 2018

page(s)

141-145

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18 February 2018

Expression of the SOX10 gene during human development

cites work

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7 January 2021

A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies

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7 January 2021

Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

Sox10, a novel transcriptional modulator in glial cells

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7 January 2021

Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently.

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

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7 January 2021

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

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7 January 2021

Differences along the place-frequency map in the structure of supporting cells in the gerbil cochlea

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7 January 2021

Induction of melanocyte-specific microphthalmia-associated transcription factor by Wnt-3a.

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Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

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7 January 2021

The development of the vertebrate inner ear.

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7 January 2021

From head to toes: the multiple facets of Sox proteins

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900236-9

7 January 2021

Seven new members of the Sox gene family expressed during mouse development

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7 January 2021

10.1016/S0169-328X(00)00236-9

Identifiers

DOI

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18 February 2018

1 reference

18 February 2018